Our client is a global medical device group.

Job Responsibilities:

• Responsible for the trial production, process verification, and mass production introduction during the transfer of domestic production lines.
• Optimize processes and manage production transfers based on product characteristics, and develop process documentation, including SOPs, drawings, process flowcharts, etc.
• Handle technical, process, equipment, and tooling issues during production, and analyze and improve significant production problems.
• Assist with the procurement, transfer, and acceptance of production equipment and tooling.
• Regularly prepare process reports and reports to the group company.
• Complete other tasks assigned by superior leaders.

Job Requirements:

• Good verbal and written communication skills in both Chinese and English.
• Minimum diploma qualification or higher, in mechanical, automation, materials engineering, electronic engineering, precision mechanics, or other related fields.
• Proficient in using office software.
• Over 2 years of work experience; experience in a medical device company is preferred.
• Able to travel to China for short-term business trips for work reporting and training.